The Type IV pilus (Tfp) is a virulence factor that mediates the initial contact of pathogenic Neisseria with epithelial cells. It subsequently activates signaling pathways that modulate cellular responses to infection. Attachment is mediated by static Tfp fibers. Signaling requires physical force exerted on the colonized cell by retracting fibers. Our preliminary findings indicate Tfp of commensal Neisseria also mediates attachment. However, the biology of commensal and pathogenic Neisseria Tfp differs in two major respects. 1) Tfp genes encoding the attachment and retraction components are under different transcriptional regulation. 2) Tfp retraction activates different signaling cascades in te epithelial cell. We hypothesize Tfp is a switch that determines whether Neisseria colonization leads to commensalism (asymptomatic colonization) or pathogenesis. This is analogous to a railroad switch at a junction that directs a train (bacterium) down tracks leading to different destinations (commensalism or pathogenesis). We further hypothesize the Tfp switching mechanism consists of two critical components: transcriptional regulation of its machinery genes, and its epithelial cell signaling activities. Transcriptional regulation determines when and where Tfp-mediated attachment and retraction occur. The types of signaling cascades activated in the host cell determine the outcome of colonization. We propose two Aims to test this hypothesis.

Public Health Relevance

The goal of this project is to determine how the Type IV pilus, a key surface structure common to commensal and pathogenic species of Neisseria, determines whether bacterial colonization leads to commensalism or pathogenesis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI107966-03
Application #
8892061
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Hiltke, Thomas J
Project Start
2013-08-08
Project End
2016-07-31
Budget Start
2015-08-01
Budget End
2016-07-31
Support Year
3
Fiscal Year
2015
Total Cost
Indirect Cost
Name
University of Arizona
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
806345617
City
Tucson
State
AZ
Country
United States
Zip Code
85721
Rendón, María A; Lona, Beatriz; Ma, Mancheong et al. (2018) RpoN and the Nps and Npa two-component regulatory system control pilE transcription in commensal Neisseria. Microbiologyopen :e00713
Hockenberry, Alyson M; Post, Deborah M B; Rhodes, Katherine A et al. (2018) Perturbing the acetylation status of the Type IV pilus retraction motor, PilT, reduces Neisseria gonorrhoeae viability. Mol Microbiol 110:677-688
Hockenberry, Alyson M; Hutchens, Danielle M; Agellon, Al et al. (2016) Attenuation of the Type IV Pilus Retraction Motor Influences Neisseria gonorrhoeae Social and Infection Behavior. MBio 7:
Paluch, Ewa K; Nelson, Celeste M; Biais, Nicolas et al. (2015) Mechanotransduction: use the force(s). BMC Biol 13:47
Rendón, María A; Hockenberry, Alyson M; McManus, Steven A et al. (2013) Sigma factor RpoN (?54) regulates pilE transcription in commensal Neisseria elongata. Mol Microbiol 90:103-13